Liquid/Solid Interface of Ultrathin Ionic Liquid Films: [C1C1lm][Tf2N] and [C8C1Im][Tf2N) on Au(111)

被引:191
作者
Cremer, T.
Stark, M.
Deyko, A.
Steinrueck, H. -P.
Maier, F. [1 ]
机构
[1] Univ Erlangen Nurnberg, Lehrstuhl Phys Chem 2, D-91058 Erlangen, Germany
关键词
SUM-FREQUENCY GENERATION; RAY PHOTOELECTRON-SPECTROSCOPY; DOUBLE-LAYER; ELECTRONIC-STRUCTURE; SURFACE-COMPOSITION; IN-VACUO; DEPOSITION; PHOTOEMISSION; ELECTROLYTES; VAPORIZATION;
D O I
10.1021/la105007c
中图分类号
O6 [化学];
学科分类号
070301 [无机化学];
摘要
Ultrathin films of two imidazolium-based ionic liquids (IL), [C(1)C(1)Im][Tf2N] (= 1,3-dimethylimidazolium bis(trifluoromethyl)imide) and [C(8)C(1)Im][Tf2N] (= 1-methyl-3-octylimidazolium bis(trifluoromethyl)imide) were prepared on a Au(111) single-crystal surface by physical vapor deposition in ultrahigh vacuum. The adsorption behavior, orientation, and growth were monitored via angle-resolved X-ray photoelectron spectroscopy (ARXPS). Coverage-dependent chemical shifts of the IL-derived core levels indicate that for both ILs the first layer is formed from anions and cations directly in contact with the Au surface in a checkerboard arrangement and that for [C(8)C(1)Im][Tf2N] a reorientation of the alkyl chain with increasing coverage is found. For both ILs, geometry models of the first adsorption layer are proposed. For higher coverages, both ILs grow in a layer-by-layer fashion up to thicknesses of at least 9 nm (>10 ML) Moreover, beam damage effects are discussed, which are mainly related to the decomposition of [Tf2N](-) anions directly adsorbed at the gold surface.
引用
收藏
页码:3662 / 3671
页数:10
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